| Identification | Back Directory | [Name]
Ethanone, 1-(3-hydroxy-2-pyridinyl)- (9CI) | [CAS]
13210-29-2 | [Synonyms]
2-Acetyl-3-hydroxypyridine
1-(3-hydroxy-2-pyridyl)ethanone
1-(3-hydroxy-2-pyridinyl)- (9CI)
1-(3-hydroxypyridin-2-yl)ethan-1-one
Ethanone, 1-(3-hydroxy-2-pyridinyl)-
Ethanone, 1-(3-hydroxy-2-pyridinyl)- (9CI)
Ethanone, 1-(3-hydroxy-2-pyridinyl)- (9CI) ISO 9001：2015 REACH | [Molecular Formula]
C7H7NO2 | [MDL Number]
MFCD08062669 | [MOL File]
13210-29-2.mol | [Molecular Weight]
137.14 |
| Chemical Properties | Back Directory | [Boiling point ]
311.5±22.0 °C(Predicted) | [density ]
1.217 | [storage temp. ]
Inert atmosphere,Room Temperature | [pka]
5.76±0.10(Predicted) | [Appearance]
Light yellow to light brown Solid |
| Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 1-(3-hydroxypyridin-2-yl)ethanone from methylmagnesium bromide and 2-cyano-3-hydroxypyridine: Referring to the method of Example 58, to a solution of tetrahydrofuran (THF, 50 mL) of 2-cyano-3-hydroxypyridine (3.00 g, 25.0 mmol) was added slowly, under cooling in an ice bath, a THF solution of 3M methylmagnesium bromide ( 25 mL). After addition, the reaction mixture was stirred at room temperature for 30 min. Subsequently, the reaction mixture was neutralized with 6N hydrochloric acid solution and extracted twice with ethyl acetate. The organic layers were combined, washed with saturated sodium chloride solution and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure to afford the title compound 1-(3-hydroxypyridin-2-yl)ethanone (3.43 g, quantitative yield) as a powdered solid. The crude product was used directly in the subsequent reaction without further purification. | [References]
[1] Patent: EP2123652, 2009, A1. Location in patent: Page/Page column 63
[2] Patent: US2017/145026, 2017, A1. Location in patent: Paragraph 0622; 0623 |
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